Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs739496
SH2B3 ; ATXN2
0.790 0.160 12 111449855 3 prime UTR variant A/G snv 0.27 3
rs540639423
SH2B3
12 111407152 intron variant C/T snv 4.6E-03 2
rs148636776
ATXN2 ; SH2B3
0.790 0.280 12 111447491 missense variant G/A snv 1.5E-04 2.4E-04 1
rs11065898
SH2B3
1.000 0.040 12 111424771 intron variant C/T snv 0.21 1
rs3803170
SH2B3
12 111409936 intron variant A/G snv 0.38 1
rs11065904
SH2B3 ; ATXN2
0.882 0.080 12 111449163 3 prime UTR variant T/A snv 3.2E-02 1